A real-world disproportionality analysis of FDA adverse event reporting system (FAERS) events for lecanemab

BackgroundLecanemab is a humanized murine IgG1 antibody. Recent Phase 3 clinical trials have demonstrated its ability to reduce brain amyloid-β (Aβ) load and slow cognitive decline in patients with early Alzheimer’s disease (AD). However, since its approval, reports on adverse effects (AEs) associat...

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Bibliographic Details
Main Authors: Linlin Yan, Linhai Zhang, Zucai Xu, Zhong Luo
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-04-01
Series:Frontiers in Pharmacology
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Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2025.1559447/full
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